Transmission Fluorometer

• US 20090312616A1
• Filed: 06/12/2009
• Published: 12/17/2009
• Est. Priority Date: 06/12/2008
• Status: Active Grant

• Current Assignee: William Paseman
• Original Assignee: Sabrina Paseman, William G. Paseman
• Inventors: Paseman, Sabrina, Paseman, William G.
• Granted Patent: US 8,306,594 B2
• Time in Patent Office: Days
• US Class Current: 600/322
• CPC Class Codes: A61B 5/0059 using light, e.g. diagnosis by transillumination, diascopy, fluorescence A61B5/0093, A61B5/1455, A61B5/02416 and A61B5/0261 take precedence
• CPC Class Codes: A61B 5/14546 for measuring analytes not otherwise provided for, e.g. ions, cytochromes
• CPC Class Codes: A61B 5/14551 for measuring blood gases
• CPC Class Codes: A61B 5/14552 Details of sensors specially adapted therefor
• CPC Class Codes: A61B 5/6825 Hand

Abstract

This disclosure relates generally to a system and method for noninvasive, non-destructive fluorescent measurement. More specifically, the disclosure provides a non-invasive metrology system and method to monitor levels of fluorescent chemicals in the blood. A major application for the invention is field-based non-invasive blood testing for micro-nutrient deficiency and diseases resulting from it, such as Iron deficient anemia. The invention may help reduce or eliminate the need for blood drawing, sending the sample to a blood lab and having to wait for a result.

Claims

1. A non-invasive measurement system for determining ratios of concentrations of at least two analytes of a sample, the system comprising:

a light source configured to provide an output spectrum which excites the at least two analytes;

receiving optics positioned relative to the light source so as to capture fluoresced light emitted by the at least two analytes upon excitation by the light source;

a spectrometric assembly capable of performing quantitative measurements of intensity and wavelength of the fluoresced light emitted by the at least two analytes upon excitation by the light source, wherein the input of the spectrometric assembly is connected to the output of the receiving optics; and

a computer system linked to the spectrometric assembly, the computer system comprising computer readable code for computing and providing as output the ratio of the concentration of one analyte relative to the concentration of at least another analyte

2. The system of claim 1 wherein the light source comprises an LED, laser diode or monochromator.

3. The system of claim 1 wherein the light source emits a wavelength chosen from the ranges of about 346 to about 370 nm, about 390 to about 400 nm and about 420 to about 430 nm.

4. The system of claim 1 wherein the light sources emits wavelengths that excite micro-nutrients.

5. The system of claim 1, further comprising a source-receiver assembly configured to maintain optical alignment between the light source and the receiving optics, whereby the sample is pinched between the light source and the receiving optics.

6. The system of claim 5 further comprising a sample holding device configured to hold the sample in a source-receiver assembly between the light source and the receiving optics.

7. The system of claim 6 wherein the sample holding device is configured to pinch a sample to a thickness consistent with measurements at wavelengths chosen from the ranges of about 346 to about 370 nm, about 390 to about 400 nm and about 420 to about 430 nm.

8. The system of claim 5 wherein the source-receiver assembly is configured to receive feedback from the computer to support automatic control of the light source.

9. A method for employing the non-invasive system of claim 1, the method comprising:

applying the source-receiver assembly to the sample whereby the sample is pinched between the light source and the receiving optics;

applying power to the light source, wherein the power level of the light source is set to a level that causes the spectrometric assembly to produce an output;

transmitting the output of the spectrometric assembly to the computer system; and

running the at least one program in the computer system.

10. The method of claim 9 wherein the sample comprises in vivo skin.

11. The method of claim 10 wherein the sample is the webbing between a patient'"'"'s thumb and forefinger.

12. The system of claim 1 wherein the sample comprises in vivo skin.

13. The system of claim 1 wherein the spectrometric assembly comprises a device selected from the group consisting of a spectrometer, a filter-photomultiplier-tube combination, a filter-charged-coupled-device, and a filter-photodiode combination.

14. The system of claim 1 wherein the computer readable code comprises instructions for employing absorption-based analyte identification algorithms to detect non-fluorescing analytes.

15. The system of claim 1 wherein the computer readable code comprises instructions for employing analyte identification algorithm to detect fluorescing analytes.

16. The system of claim 1 wherein the light source comprises multiple LEDs, each LED emitting light over a different range of wavelengths.

17. The system of claim 1 wherein the receiving optics are positioned at an angle of about 180°

relative to the light source.

18. The system of claim 1 wherein the receiving optics are positioned at an angle of greater than 90°

relative to the light source.

19. The system of claim 1 wherein the computer readable code comprises instructions for computing the ratios of heights of multiple emission peaks to determine the ratio of the concentration of one analyte to the concentration of another analyte.

20. The system of claim 1 wherein the computer readable code comprises instructions for computing the ratio of one set of excitation and emission peaks to the ratio of another set of excitation and emission peaks to determine the ratio of the concentration of one analyte to the concentration of another analyte.

21. A method for non-invasively determining ratios of blood analyte concentrations, the method comprising:

pinching an in vivo skin sample between a light source and an optics system configured to receive radiation;

emitting radiation from the light source onto the skin sample, the light source being configured to provide an output spectrum that excites at least two blood analytes;

optically receiving fluoresced light emitted by the at least two blood analytes upon excitation by the light source;

measuring the intensity and wavelength of the fluoresced light emitted by the at least two blood analytes upon excitation by the light source; and

determining a ratio of the concentration of one analyte to the concentration of at least another analyte.

22. The method of claim 21 wherein the skin is the webbing between the patients thumb and forefinger.

23. The method of claim 21 wherein the skin is a section of loose skin on a subject'"'"'s wrist or elbow joint.

24. The method of claim 21 wherein the at least two analytes are compounds chosen from retinol, hemoglobin, zinc protoporphyrin, protophorphyrin IX and fluorescent heme degradation product.

25. The method of claim 21 wherein the light source comprises a wavelength chosen from the ranges of about 346 to about 370 nm, about 390 to about 400 nm and about 420 to about 430 nm.

26. The method of claim 21 wherein the measuring further comprises measuring the intensity and wavelength of the fluoresced light emitted by the at least two blood analytes upon excitation by the light source.

27. A non-invasive measurement system for determining ratios of concentrations of at least two analytes of a sample, the system comprising:

a light source configured to provide an output spectrum which excites the at least two analytes;

receiving optics positioned relative to the light source so as to capture both excitation light transmitted through the sample and fluoresced light emitted by the at least two analytes upon excitation by the light source;

a spectrometric assembly capable of performing quantitative measurements of intensity and wavelength of both excitation light transmitted through the sample and the fluoresced light emitted by the at least two analytes upon excitation by the light source, wherein the input of the spectrometric assembly is connected to the output of the receiving optics; and

a computer system linked to the spectrometric assembly, the computer system comprising computer readable code for computing and providing as output the ratio of the concentration of one analyte relative to the concentration of at least another analyte.

28. The system of claim 27 wherein the light source comprises an LED, laser diode or monochromator.

29. The system of claim 27 wherein the light source emits a wavelength chosen from the ranges of about 346 to about 370 nm, about 390 to about 400 nm and about 420 to about 430 nm.

30. The system of claim 27 further comprising a source-receiver assembly configured to maintain optical alignment between the light source and the receiving optics, whereby the sample is pinched between the light source and the receiving optics.

31. The system of claim 27 wherein the sample comprises in vivo skin.

32. The system of claim 27 wherein the computer readable code comprises instructions for employing absorption-based analyte identification algorithms to detect non-fluorescing analytes.

33. The system of claim 27 wherein the computer readable code comprises instructions for employing analyte identification algorithm to detect fluorescing analytes.

34. The system of claim 27 wherein the light source comprises multiple LEDs, each LED emitting light over a different range of wavelengths.

35. The system of claim 27 wherein the computer readable code comprises instructions for computing the ratio of one set of excitation and emission peaks to the ratio of another set of excitation and emission peaks to determine the ratio of the concentration of one analyte relative to the concentration of another analyte.